Substrates for peptidase M01.020: tricorn interacting factor F2

Summary Alignment Tree Sequences Sequence features Distribution Literature Substrates

Peptide and protein substrates that are thought to be physiologically relevant are indicated by P. Peptide and protein substrates that are thought to be pathologically relevant are indicated by D. Peptide and protein substrates that are not physiologically relevant are indicated by N. Synthetic substrates are indicated by S. Click on the symbol to show only physiological, non-physiological or synthetic substrates, or here to display all substrates. How cleavage sites have been identified are indicated by the following evidence codes: NT = N-terminal sequencing, MS = mass spectroscopy, MU = mutation, CS = consensus sequence, LC = liquid chromatography. To see all annotated cleavages for a protein substrate, click on the UniProt Accession.

Substrate Uniprot Residue range Cleavage Site Cleavage type Evidence P4 P3 P2 P1 P1' P2' P3' P4' Reference CutDB MERNUM
Ala-NHMec Ala+NHMec S - - - Ala AMC - - - Tamura & Baumeister, 2004
Arg-NHMec Arg+NHMec S - - - Arg AMC - - - Tamura & Baumeister, 2004
Leu-NHMec Leu+NHMec S - - - Leu AMC - - - Tamura & Baumeister, 2004
Phe-NHMec Phe+NHMec S - - - Phe AMC - - - Tamura & Baumeister, 2004
Pro-NHMec Pro+NHMec S - - - Pro AMC - - - Tamura et al., 1998
Tyr-NHMec Tyr+NHMec S - - - Tyr AMC - - - Tamura & Baumeister, 2004